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array:23 [ "pii" => "S1413867023000053" "issn" => "14138670" "doi" => "10.1016/j.bjid.2023.102745" "estado" => "S300" "fechaPublicacion" => "2023-03-01" "aid" => "102745" "copyright" => "Sociedade Brasileira de Infectologia" "copyrightAnyo" => "2023" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Braz J Infect Dis. 2023;27:" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "itemSiguiente" => array:18 [ "pii" => "S1413867023000041" "issn" => "14138670" "doi" => "10.1016/j.bjid.2023.102743" "estado" => "S300" "fechaPublicacion" => "2023-03-01" "aid" => "102743" "copyright" => "Sociedade Brasileira de Infectologia" "documento" => "article" "crossmark" => 1 "subdocumento" => "rev" "cita" => "Braz J Infect Dis. 2023;27:" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Review Article</span>" "titulo" => "Epoxy-α-lapachone (2,2-Dimethyl-3,4-dihydro-spiro[2H-naphtho[2,3-b]pyran-10,2′-oxirane]-5(10H)-one): a promising molecule to control infections caused by protozoan parasites" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => "en" "contieneResumen" => array:1 [ "en" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig0002" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 916 "Ancho" => 2000 "Tamanyo" => 136105 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "alt0002" "detalle" => "Fig " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spara002" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Predicted epoxy-α-lapachone regions interactions with amino acid residues of the active site of trypanosomatid proteases.</span> Epoxy-α-lapachone (2,3-Dihydro-3,3-dimethylspiro[1H-4-oxanthracene-5,2′-oxiran]−10(5H)-one) is formed by an aromatic ring (A), a central six-membered ring (B) and a ring with two methyl groups (C). The chiral center being the C12 atom, which is also part of the three-membered epoxide ring.<a class="elsevierStyleCrossRef" href="#bib0044"><span class="elsevierStyleSup">44</span></a> CID: 12,000,280; molecular formula:C<span class="elsevierStyleInf">16</span>H<span class="elsevierStyleInf">16</span>O<span class="elsevierStyleInf">3</span> and molecular mass: 256.3 g/mol. Epoxy-α-lapachone regions interactions with amino acid residues of cysteine-proteinase (green) of <span class="elsevierStyleItalic">Trypanosoma cruzi</span><a class="elsevierStyleCrossRef" href="#bib0048"><span class="elsevierStyleSup">48</span></a> and serine-proteinase (orange) of <span class="elsevierStyleItalic">Leishmania</span> (<span class="elsevierStyleItalic">Leishmania</span>) <span class="elsevierStyleItalic">amazonensis</span>.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">50</span></a></p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Juliana Figueiredo Peixoto, Adriane da Silva Oliveira, Luiz Filipe Gonçalves - Oliveira, Franklin Souza - Silva, Carlos Roberto Alves" "autores" => array:5 [ 0 => array:2 [ "nombre" => "Juliana Figueiredo" "apellidos" => "Peixoto" ] 1 => array:2 [ "nombre" => "Adriane da Silva" "apellidos" => "Oliveira" ] 2 => array:2 [ "nombre" => "Luiz Filipe" "apellidos" => "Gonçalves - Oliveira" ] 3 => array:2 [ "nombre" => "Franklin" "apellidos" => "Souza - Silva" ] 4 => array:2 [ "nombre" => "Carlos Roberto" "apellidos" => "Alves" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1413867023000041?idApp=UINPBA00003Y" "url" => "/14138670/0000002700000002/v3_202304071918/S1413867023000041/v3_202304071918/en/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S1413867023000065" "issn" => "14138670" "doi" => "10.1016/j.bjid.2023.102746" "estado" => "S300" "fechaPublicacion" => "2023-03-01" "aid" => "102746" "copyright" => "Sociedade Brasileira de Infectologia" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Braz J Infect Dis. 2023;27:" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "en" => array:10 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Chronic medical conditions associated with invasive pneumococcal diseases in inpatients in teaching hospitals in São Paulo city: Estimating antimicrobial susceptibility and serotype-coverage of pneumococcal vaccines" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => "en" "contieneResumen" => array:1 [ "en" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Renato A. Kfouri, Maria-Cristina C. Brandileone, Marco Aurélio P. Sáfadi, Rosana Richtmann, Alfredo E. Gilio, Flavia Rossi, Thais Guimarães, Ana Luiza Bierrenbach, José C. Moraes" "autores" => array:10 [ 0 => array:2 [ "nombre" => "Renato A." "apellidos" => "Kfouri" ] 1 => array:2 [ "nombre" => "Maria-Cristina C." "apellidos" => "Brandileone" ] 2 => array:2 [ "nombre" => "Marco Aurélio P." "apellidos" => "Sáfadi" ] 3 => array:2 [ "nombre" => "Rosana" "apellidos" => "Richtmann" ] 4 => array:2 [ "nombre" => "Alfredo E." "apellidos" => "Gilio" ] 5 => array:2 [ "nombre" => "Flavia" "apellidos" => "Rossi" ] 6 => array:2 [ "nombre" => "Thais" "apellidos" => "Guimarães" ] 7 => array:2 [ "nombre" => "Ana Luiza" "apellidos" => "Bierrenbach" ] 8 => array:2 [ "nombre" => "José C." "apellidos" => "Moraes" ] 9 => array:1 [ "colaborador" => "São Paulo Study Group for IPD" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1413867023000065?idApp=UINPBA00003Y" "url" => "/14138670/0000002700000002/v3_202304071918/S1413867023000065/v3_202304071918/en/main.assets" ] "en" => array:17 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Safety of levofloxacin as an antibiotic prophylaxis in the induction phase of children newly diagnosed with acute lymphoblastic leukemia: an interim analysis of a randomized, open-label trial in Brazil" "tieneTextoCompleto" => true "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Mauro Cesar Dufrayer, Ciliana Rechenmacher, Clarice Franco Meneses, Yasmine Massaro Carneiro Monteiro, Fabianne Altruda de Moraes Costa Carlesse, Fabrizio Motta, Liane Esteves Daudt, Mariana Bohns Michalowski" "autores" => array:8 [ 0 => array:4 [ "nombre" => "Mauro Cesar" "apellidos" => "Dufrayer" "email" => array:1 [ 0 => "mauro.dufrayer@santacasa.org.br" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0001" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0001" ] ] ] 1 => array:3 [ "nombre" => "Ciliana" "apellidos" => "Rechenmacher" "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0003" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">e</span>" "identificador" => "aff0005" ] ] ] 2 => array:3 [ "nombre" => "Clarice Franco" "apellidos" => "Meneses" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0002" ] ] ] 3 => array:3 [ "nombre" => "Yasmine Massaro Carneiro" "apellidos" => "Monteiro" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0003" ] ] ] 4 => array:3 [ "nombre" => "Fabianne Altruda de Moraes Costa" "apellidos" => "Carlesse" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">d</span>" "identificador" => "aff0004" ] ] ] 5 => array:3 [ "nombre" => "Fabrizio" "apellidos" => "Motta" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0001" ] ] ] 6 => array:3 [ "nombre" => "Liane Esteves" "apellidos" => "Daudt" "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0002" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0003" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">e</span>" "identificador" => "aff0005" ] ] ] 7 => array:3 [ "nombre" => "Mariana Bohns" "apellidos" => "Michalowski" "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0002" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0003" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">e</span>" "identificador" => "aff0005" ] ] ] ] "afiliaciones" => array:5 [ 0 => array:3 [ "entidad" => "Hospital da Criança Santo Antônio, Porto Alegre, RS, Brazil" "etiqueta" => "a" "identificador" => "aff0001" ] 1 => array:3 [ "entidad" => "Hospital de Clínicas de Porto Alegre (HCPA), Serviço de Oncologia Pediátrica, Porto Alegre, RS, Brazil" "etiqueta" => "b" "identificador" => "aff0002" ] 2 => array:3 [ "entidad" => "Universidade Federal do Rio Grande do Sul (UFRGS), Departamento de Pediatria, Porto Alegre, RS, Brazil" "etiqueta" => "c" "identificador" => "aff0003" ] 3 => array:3 [ "entidad" => "Universidade Federal de São Paulo (UNIFESP), Instituto de Oncologia Pediátrica – GRAACC, São Paulo, SP, Brazil" "etiqueta" => "d" "identificador" => "aff0004" ] 4 => array:3 [ "entidad" => "Hospital de Clínicas de Porto Alegre (HCPA), Laboratório de Pediatria Translacional, Serviço de Pesquisa Experimental, Porto Alegre, RS, Brazil" "etiqueta" => "e" "identificador" => "aff0005" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0001" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0001" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0007">Introduction</span><p id="para0005" class="elsevierStylePara elsevierViewall">Malignant neoplasms are the leading cause of disease-related childhood deaths and, among them, acute lymphoblastic leukemias (ALLs) are the most prevalent.<a class="elsevierStyleCrossRef" href="#bib0001"><span class="elsevierStyleSup">1</span></a> ALLs can be defined as a heterogeneous group of diseases manifested by the proliferation of immature lymphoblasts in the marrow, in peripheral blood or on other tissues. It is basically treated with high-dose polychemotherapy, followed by a maintenance phase consisting of low-dose chemotherapy.<a class="elsevierStyleCrossRef" href="#bib0002"><span class="elsevierStyleSup">2</span></a></p><p id="para0006" class="elsevierStylePara elsevierViewall">Despite the positive evolution of treatment over the last decades –with a global survival rate close to 90%<a class="elsevierStyleCrossRef" href="#bib0003"><span class="elsevierStyleSup">3</span></a> – treatment-related mortality (TRM) remains significant: about 4% of patients die during remission induction therapy. Approximately two-thirds of these deaths are due to infectious causes.<a class="elsevierStyleCrossRef" href="#bib0004"><span class="elsevierStyleSup">4</span></a></p><p id="para0007" class="elsevierStylePara elsevierViewall">Bacteria can thus be perceived as one of the main causative agents of morbidity and mortality in patients with chemotherapy-related neutropenia. In adults, significant benefits were demonstrated with the use of antibiotic prophylaxis during these periods, as they reduced infections and lowered rates of infection-related mortality.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">5</span></a> While the use of antibiotic prophylaxis in adult patients during periods of afebrile neutropenia is already a well-established practice, we lack solid evidence concerning its use in children.</p><p id="para0008" class="elsevierStylePara elsevierViewall">Levofloxacin, a broad-spectrum fluoroquinolone antibiotic, is included in guidelines and indicated to afebrile neutropenic adult patients. According to a recommendation published by The Infectious Diseases Society of America (IDSA) in July 2020, the regular use of antibiotic prophylaxis for children with <span class="elsevierStyleItalic">de novo</span> ALL is not indicated during the induction phase precisely because of the low body of evidence that exists. When necessary, the IDSA suggests levofloxacin as the antibiotic of choice and only for patients with severe neutropenia (absolute neutrophil count < 500/mm<span class="elsevierStyleSup">3</span>) for at least seven days.<a class="elsevierStyleCrossRef" href="#bib0006"><span class="elsevierStyleSup">6</span></a></p><p id="para0009" class="elsevierStylePara elsevierViewall">In spite of the scarcity of currently available information, a few observational studies on the use of levofloxacin and one randomized trial in children with relapsed ALL have been published. Wolf et al. demonstrated that levofloxacin reduced the odds of febrile neutropenia, bacterial infection, and bloodstream infection during the induction therapy of children with LLA. Surprisingly, it also reduced the chances of infections from <span class="elsevierStyleItalic">C. difficile</span> without breakthrough infections with antibiotic-resistant organisms.<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> Similarly, Sulis et al. verified that the use of Fluoroquinolones (levofloxacin or moxifloxacin) for prophylaxis in children with an initial diagnosis of ALL receiving induction chemotherapy was effective in reducing Gram-negative and some Gram-positive bacteremia. Moreover, no increased incidence of multidrug-resistant microorganism, <span class="elsevierStyleItalic">C. difficile</span> infection, or fungi was observed.<a class="elsevierStyleCrossRef" href="#bib0008"><span class="elsevierStyleSup">8</span></a></p><p id="para0010" class="elsevierStylePara elsevierViewall">Considering the promising activity of levofloxacin in preventing febrile neutropenia and the lack of knowledge regarding its possible adverse effects in the induction phase, we conducted the present study to assess the safety and efficacy of this antibiotic medication in children newly-diagnosed with ALL during the induction phase. This preliminary interim analysis aims to ensure greater safety for the patients contemplated in this study and allows the continuation of the clinical trial.</p></span><span id="sec0002" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0008">Material and methods</span><span id="sec0003" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0009">Trial design, oversight, and participants</span><p id="para0011" class="elsevierStylePara elsevierViewall">From May 2021 to June 2022, children aged one through 18 years, with newly-diagnosed ALL admitted at three pediatric oncology centers in Brazil, who completed induction therapy before 30 June 2022, were enrolled in this multicenter, open label, randomized, phase 3 clinical trial. Children with any type of allergy to the use of quinolones and a history of chronic arthritis undergoing treatment were not included in the study. Children with clinically or microbiologically documented infection prior to initiation of induction, as well as those with fever prior to induction therapy that required prolonged antibiotic therapy (> 5 days) to treat infection, were not included in the study in order to avoid confounding antibiotic treatment with antibiotic prophylaxis. Likewise, children with any form of allergy to quinolones or with a history of chronic arthritis treatment were not included in this trial. Patients who developed febrile neutropenia within the first seven days of induction or after up to two days of neutropenia were excluded due to the lack of sufficient time for antibiotic prophylaxis activity.</p><p id="para0012" class="elsevierStylePara elsevierViewall">The trial protocol was approved by the ethics committee or institutional review board at each of the participating centers (CAAE 43,076,621.8.2001.5683). The children's parents or legally acceptable representatives provided written informed consent.</p></span><span id="sec0004" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0010">Randomization</span><p id="para0013" class="elsevierStylePara elsevierViewall">Eligible patients were randomly assigned in a 1:1 ratio by a computer-generated number. During the induction phase, patients would either be given levofloxacin (intervention group) as a prophylactic agent or no prophylaxis (control group).</p></span><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0011">Treatment</span><p id="para0014" class="elsevierStylePara elsevierViewall">All patients were treated according to the IC-BFM 2009 chemotherapy protocol. Patients in the intervention group started using levofloxacin on the third day after the beginning of induction and its use was continued until any of the following criteria were met: (a) absolute neutrophil count greater than or equal to 500/μL after nadir; (b) start of the next cycle of chemotherapy; (c) use of parenteral antibiotic therapy for any reason.</p><p id="para0015" class="elsevierStylePara elsevierViewall">Children aged 1 to < 5 years were given a dose of 10 mg/kg/dose of levofloxacin, twice a day; children older than five years were prescribed 10 mg/kg/dose once a day, with a maximum dose of 750 mg a day. Levofloxacin was administered orally but, if the oral route was not tolerated, it could be administered intravenously at the same dose and schedule.</p><p id="para0016" class="elsevierStylePara elsevierViewall">Although the control group did not receive levofloxacin as primary prophylaxis, both groups received trimethoprim-sulfamethoxazole as primary prophylaxis for <span class="elsevierStyleItalic">Pneumocystis jirovecii</span>.</p><p id="para0017" class="elsevierStylePara elsevierViewall">All patients from both groups received induction therapy that included four weeks of oral prednisone, fours weekly doses of vincristine, two or four weekly doses of daunorubicin, and two doses of PEG-asparaginase.</p></span><span id="sec0006" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0012">Outcomes and assessments</span><p id="para0018" class="elsevierStylePara elsevierViewall">The primary endpoints were CPE colonization, <span class="elsevierStyleItalic">C. difficile</span> diarrhea, and adverse events related to the use of levofloxacin. The second endpoint was febrile neutropenia during induction.</p><p id="para0019" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">C. difficile</span> diarrhea was defined by the presence of diarrhea and identification of <span class="elsevierStyleItalic">C. difficile</span> in stools by PCR or presence of its toxins.</p><p id="para0020" class="elsevierStylePara elsevierViewall">CPE colonization monitoring was performed by rectal swab at the time of admission to the hospital and at the end of the induction phase. Any additional swab collection was at the discretion of the physician or Hospital Infection Control team of each center.</p><p id="para0021" class="elsevierStylePara elsevierViewall">Febrile neutropenia was defined by the presence of axillary body temperature greater than or equal to 37.8 °C in patients whose total neutrophil count was below 500/μL.</p><p id="para0022" class="elsevierStylePara elsevierViewall">Adverse effects were defined in terms of causality and classified as: possible, likely, or certain. They were also described regarding the severity of each physiological system and classified as: mild, moderate, severe or fatal, according to modified criteria of the World Health Organization (<a class="elsevierStyleCrossRef" href="#tbl0001">Tables 1</a> and <a class="elsevierStyleCrossRef" href="#tbl0002">2</a>).<a class="elsevierStyleCrossRef" href="#bib0009"><span class="elsevierStyleSup">9</span></a></p><elsevierMultimedia ident="tbl0001"></elsevierMultimedia><elsevierMultimedia ident="tbl0002"></elsevierMultimedia></span><span id="sec0007" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0013">Statistical methods</span><p id="para0023" class="elsevierStylePara elsevierViewall">This study is ongoing and data for this interim analysis were collected on June 23, 2022 after 18 months of initiation. Efficacy and safety analyses included all patients who completed induction phase chemotherapy. Initial target enrollment for the main cohort of the study was 196 patients for the outcome febrile neutropenia, 98 in each group.</p><p id="para0024" class="elsevierStylePara elsevierViewall">Qualitative variables were summarized as absolute and relative frequencies and differences were considered significant at <span class="elsevierStyleItalic">p</span> < 0.05 (2-tailed). Data were compiled using the REDCap® web application and analyzed using the PASW Statistics Version 18.0. Fisher's exact test and Pearson's chi-square test were used for categorical variables, and the Mann–Whitney U test for quantitative variables. The binomial proportion confidence interval for the occurrence of adverse events was calculated using the Clopper-Pearson interval.</p></span></span><span id="sec0008" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0014">Results</span><p id="para0025" class="elsevierStylePara elsevierViewall">Twenty patients were included in the interim analysis: Ten in the control group and 10 in the intervention group, who received prophylaxis with levofloxacin. <a class="elsevierStyleCrossRef" href="#tbl0003">Table 3</a> shows the characteristics of each group. The median follow-up was 289 days (27 - 394 days). The median duration of levofloxacin use was 29 days (23 - 37 days).</p><elsevierMultimedia ident="tbl0003"></elsevierMultimedia><p id="para0026" class="elsevierStylePara elsevierViewall">Only one death, due to sepsis by <span class="elsevierStyleItalic">Pseudomonas aeruginosa,</span> was observed in the control group. The patient was a male with Down syndrome who died on the thirtieth day of induction. Among the 10 patients who received levofloxacin, three had adverse reactions classified as mild and probably related to levofloxacin. Two patients suffered from nausea, so it was necessary to switch administration of medication from oral to intravenous with cessation of symptoms. One (1) patient had a transient increase in hepatic transaminases, reaching levels up to five times the upper level of normality. Interruption of levofloxacin was not necessary (<a class="elsevierStyleCrossRef" href="#tbl0004">Table 4</a>).</p><elsevierMultimedia ident="tbl0004"></elsevierMultimedia><p id="para0027" class="elsevierStylePara elsevierViewall">Three patients had <span class="elsevierStyleItalic">C. difficile</span> diarrhea, two in the levofloxacin group and one in the control group (<span class="elsevierStyleItalic">p</span> > 0.99). Only one patient assigned to the levofloxacin group presented colonization by CPE in this study identified as <span class="elsevierStyleItalic">Klebsiella</span> spp. Similarly, no significant difference was observed between the groups (<span class="elsevierStyleItalic">p</span> > 0.99).</p><p id="para0028" class="elsevierStylePara elsevierViewall">Nine patients presented febrile neutropenia in the study, five in the intervention group, and four in the control group. No significant difference between groups was observed <span class="elsevierStyleItalic">(p</span> > 0.99).</p></span><span id="sec0009" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0015">Discussion</span><p id="para0029" class="elsevierStylePara elsevierViewall">In this preliminary multicenter analysis, the use of levofloxacin showed to be safe in children newly diagnosed with ALL during the induction phase. Its use did not increase the rate of colonization by CPE nor the rate of diarrhea by <span class="elsevierStyleItalic">C. difficile</span>. Despite the significant number of adverse reactions related to its use, all were mild and remitted either spontaneously or by switching administration of medication to the intravenous route.</p><p id="para0030" class="elsevierStylePara elsevierViewall">Among the few available data on the use of levofloxacin with children, a cohort study carried out in 2017 at St. Jude Children's Research Hospital (Memphis/Tennessee) with 344 patients found that prophylaxis was able to significantly prevent FN and systemic infection during induction chemotherapy by ≥70%. The use of levofloxacin in these children also minimized the use of antibiotic treatment with cefepime/ceftazidime, vancomycin, and aminoglycosides. Unexpectedly, prophylaxis with levofloxacin also dramatically reduced colitis infection rates caused by <span class="elsevierStyleItalic">Clostridioides difficile</span> and other enterocolitis. This is extremely relevant information since infection with <span class="elsevierStyleItalic">Clostridioides difficile</span> is related to higher mortality in hospitalized children, higher hospital costs, and longer hospital stays.<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a></p><p id="para0031" class="elsevierStylePara elsevierViewall">In the same year, Sulis et al. corroborated these findings by demonstrating that FQ use for the initial treatment of fever, as well as for prophylaxis in 230 children with an initial diagnosis of ALL receiving induction chemotherapy, was effective in reducing Gram-negative and some Gram-positive bacteremia. In addition, it was shown that levofloxacin did not lead to increased incidence of multiresistant microorganisms nor infections by <span class="elsevierStyleItalic">C. difficile</span> or fungi.<a class="elsevierStyleCrossRef" href="#bib0008"><span class="elsevierStyleSup">8</span></a></p><p id="para0032" class="elsevierStylePara elsevierViewall">The present study, a randomized clinical trial, is the first conducted in Brazil to assess safety and infectious outcomes with the use of levofloxacin in children with an initial diagnosis of ALL in the induction phase.</p><p id="para0033" class="elsevierStylePara elsevierViewall">Due to the history of arthropathies in animal models, the potential to induce bacterial resistance, and fluoroquinolone-resistant <span class="elsevierStyleItalic">C. difficile</span> diarrhea, an interim analysis was essential to allow the clinical trial to continue, ensuring greater safety for the observed patients.</p><p id="para0034" class="elsevierStylePara elsevierViewall">While long-term use of levofloxacin may increase the incidence of antibiotic resistance and the development of <span class="elsevierStyleItalic">C. difficile</span> diarrhea, the GIMEMA study and a recent meta-analysis of randomized controlled trials demonstrated that these potential facts did not impact infectious outcomes.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">10-12</span></a></p><p id="para0035" class="elsevierStylePara elsevierViewall">The study has some limitations. It was not powered to detect differences between the evaluated outcomes. The high number of patients admitted with fever, requiring prolonged antibiotic therapy, significantly reduced sample size. Most importantly, the study was not blinded. Awareness of allocation could affect patient care decisions.</p><p id="para0036" class="elsevierStylePara elsevierViewall">The results shown here allow for the continuity of the study, as acute toxicity or emergence of multidrug-resistant strains were not observed in the group undergoing intervention (use of FQ). Evidently, it is not possible to assess, at this time, any impact on rates of febrile neutropenia or ICU admissions, as the number of patients evaluated is insufficient to analyze these outcomes. Such aspects will be better approached at the end of the study.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:8 [ 0 => array:3 [ "identificador" => "xres1877550" "titulo" => "Abstract" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abss0001" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abss0002" "titulo" => "Methods" ] 2 => array:2 [ "identificador" => "abss0003" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abss0004" "titulo" => "Conclusion" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1628616" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "sec0001" "titulo" => "Introduction" ] 3 => array:3 [ "identificador" => "sec0002" "titulo" => "Material and methods" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0003" "titulo" => "Trial design, oversight, and participants" ] 1 => array:2 [ "identificador" => "sec0004" "titulo" => "Randomization" ] 2 => array:2 [ "identificador" => "sec0005" "titulo" => "Treatment" ] 3 => array:2 [ "identificador" => "sec0006" "titulo" => "Outcomes and assessments" ] 4 => array:2 [ "identificador" => "sec0007" "titulo" => "Statistical methods" ] ] ] 4 => array:2 [ "identificador" => "sec0008" "titulo" => "Results" ] 5 => array:2 [ "identificador" => "sec0009" "titulo" => "Discussion" ] 6 => array:2 [ "identificador" => "xack661107" "titulo" => "Funding" ] 7 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2022-08-09" "fechaAceptado" => "2023-01-05" "PalabrasClave" => array:1 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1628616" "palabras" => array:7 [ 0 => "Acute lymphoblastic leukemia" 1 => "Pediatric" 2 => "Fluoroquinolone" 3 => "Induction" 4 => "Prophylaxis" 5 => "Levofloxacin" 6 => "Febrile neutropenia" ] ] ] ] "tieneResumen" => true "resumen" => array:1 [ "en" => array:3 [ "titulo" => "Abstract" "resumen" => "<span id="abss0001" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0002">Background</span><p id="spara007" class="elsevierStyleSimplePara elsevierViewall">Despite high cure rates, treatment-related mortality in children with acute lymphoblastic leukemia (ALL) remains significant. About 4% of patients die during remission induction therapy and approximately two-thirds of treatment-related deaths are due to infectious complications.</p></span> <span id="abss0002" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0003">Methods</span><p id="spara008" class="elsevierStyleSimplePara elsevierViewall">From May 2021 to June 2022, children aged one through 18 years, with a recent diagnosis of ALL, admitted to three pediatric oncology centers in Brazil, were enrolled in this multicenter, open-label, randomized, phase 3 clinical trial. Eligible patients were randomly divided into two groups, based on a 1:1 allocation ratio, to receive, or not, levofloxacin as a prophylactic agent during the induction phase. All patients were treated according to the IC-BFM 2009 chemotherapy protocol. Primary endpoints were carbapenemase-producing Enterobacteriaceae (CPE) colonization, <span class="elsevierStyleItalic">Clostridioides difficile</span> diarrhea, and other adverse events related to the use of levofloxacin. The secondary endpoint was febrile neutropenia during induction. The median follow-up was 289 days.</p></span> <span id="abss0003" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0004">Results</span><p id="spara009" class="elsevierStyleSimplePara elsevierViewall">Twenty patients were included in this trial, 10 in each group (control and levofloxacin). Mild adverse reactions related to levofloxacin were observed in three patients (30%). Three patients had <span class="elsevierStyleItalic">Clostridioides difficile</span> diarrhea, two in the levofloxacin group and one in the control group (<span class="elsevierStyleItalic">p</span> > 0.99). Only one patient presented colonization by CPE. This patient belonged to the levofloxacin group (<span class="elsevierStyleItalic">p</span> > 0.99). Nine patients presented febrile neutropenia, five in the control group and four in the levofloxacin intervention group (<span class="elsevierStyleItalic">p</span> > 0.99), one patient died due to febrile neutropenia.</p></span> <span id="abss0004" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="cesectitle0005">Conclusion</span><p id="spara010" class="elsevierStyleSimplePara elsevierViewall">The use of levofloxacin was shown to be safe in the induction phase in children with <span class="elsevierStyleItalic">de novo</span> ALL. The use of this medication did not increase the rate of colonization by CPE nor the rate of diarrhea by <span class="elsevierStyleItalic">C. difficile</span>. All adverse reactions were mild and remitted either spontaneously or after switching medicine administration from oral to intravenous route.</p></span>" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abss0001" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abss0002" "titulo" => "Methods" ] 2 => array:2 [ "identificador" => "abss0003" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abss0004" "titulo" => "Conclusion" ] ] ] ] "multimedia" => array:4 [ 0 => array:8 [ "identificador" => "tbl0001" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "alt0001" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:1 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><a name="en0001"></a><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="" valign="top">Possible \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0002"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Occurs where two or more medications may be involved, or it can be inferred relationship with the disease \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0003"></a><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="" valign="top">Likely \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0004"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Occurs where only one drug may be involved \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0005"></a><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="" valign="top">Certain \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0006"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Occurs during infusion and/or re-exposure \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spara001" class="elsevierStyleSimplePara elsevierViewall">WHO classification of toxicity as causality.</p>" ] ] 1 => array:8 [ "identificador" => "tbl0002" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "alt0002" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:1 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><a name="en0007"></a><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="" valign="top">Mild \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0008"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Small clinical and short-term importance, which may require treatment, not substantially affecting the patient's life \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0009"></a><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="" valign="top">Moderate \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0010"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Alters the patient's usual activities, resulting in transient disability without sequelae. Needs intervention \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0011"></a><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="" valign="top">Severe \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0012"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Directly threatens the patient's life, causes hospitalization, and can cause permanent sequelae \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0013"></a><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="" valign="top">Fatal \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0014"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Results in death \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spara002" class="elsevierStyleSimplePara elsevierViewall">WHO Classification of toxicity as severity.</p>" ] ] 2 => array:8 [ "identificador" => "tbl0003" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "alt0003" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:3 [ "leyenda" => "<p id="spara004" class="elsevierStyleSimplePara elsevierViewall">Abbreviations. ALL, acute lymphoblastic leukemia; IQR, interquartile range; y, year(s).</p>" "tablatextoimagen" => array:1 [ 0 => array:1 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><a name="en0015"></a><th class="td-with-role" title="\n \t\t\t\t\ttable-head\n \t\t\t\t ; entry_with_role_colgroup " colspan="4" align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Patients, No (%)<a class="elsevierStyleCrossRef" href="#tb3fn1"><span class="elsevierStyleSup">a</span></a></th></tr><tr title="table-row"><a name="en0016"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black">Characteristics \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0017"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black">No Prophylaxis (<span class="elsevierStyleItalic">n</span> = 10) \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0018"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black">Levofloxacin (<span class="elsevierStyleItalic">n</span> = 10) \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0019"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">p-</span>Value<a class="elsevierStyleCrossRef" href="#tb3fn2"><span class="elsevierStyleSup">b</span></a> \t\t\t\t\t\t\n \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><a name="en0024a"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Age, median (IQR), y \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0025a"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">8.0 (2–13.5) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0022"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">9.5 (2–14.0) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0023"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">.971 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0024"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Sex \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0025"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0026"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0027"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">>0.99 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0028"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"><span class="elsevierStyleHsp" style=""></span>Male \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0029"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">6 (60) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0030"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">7 (70) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0031"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0032"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"><span class="elsevierStyleHsp" style=""></span>Female \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0033"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">4 (40) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0034"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">3 (30) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0035"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0036"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Down Syndrome \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0037"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">1 (10) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0038"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">1 (10) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0039"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">>0.99 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0040"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">ALL type \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0041"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0042"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0043"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">>0.99 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0044"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"><span class="elsevierStyleHsp" style=""></span>B \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0045"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">8 (80) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0046"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">9 (90) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0047"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0048"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"><span class="elsevierStyleHsp" style=""></span>T \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0049"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">2 (20) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0050"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">1 (10) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0051"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] ] ] "notaPie" => array:2 [ 0 => array:3 [ "identificador" => "tb3fn1" "etiqueta" => "a" "nota" => "<p class="elsevierStyleNotepara" id="notep0002">Data represent No. (%) of patients except otherwise specified.</p>" ] 1 => array:3 [ "identificador" => "tb3fn2" "etiqueta" => "b" "nota" => "<p class="elsevierStyleNotepara" id="notep0003">Fisher's exact test was used for categorical variables and the Mann–Whitney U test for quantitative variables.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spara003" class="elsevierStyleSimplePara elsevierViewall">Characteristics of the patients included in the analysis.</p>" ] ] 3 => array:8 [ "identificador" => "tbl0004" "etiqueta" => "Table 4" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "alt0004" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:3 [ "leyenda" => "<p id="spara006" class="elsevierStyleSimplePara elsevierViewall">CPE, carbapenemase-producing Enterobacteriaceae; AEs, adverse events.</p>" "tablatextoimagen" => array:1 [ 0 => array:1 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><a name="en0052"></a><th class="td-with-role" title="\n \t\t\t\t\ttable-head\n \t\t\t\t ; entry_with_role_colgroup " colspan="5" align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Patients, No (%)</th></tr><tr title="table-row"><a name="en0053"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col"> \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0054"></a><th class="td-with-role" title="\n \t\t\t\t\ttable-head\n \t\t\t\t ; entry_with_role_colgroup " colspan="2" align="left" valign="top" scope="col" style="border-bottom: 2px solid black">No Prophylaxis</th><a name="en0055"></a><th class="td-with-role" title="\n \t\t\t\t\ttable-head\n \t\t\t\t ; entry_with_role_colgroup " colspan="2" align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Levofloxacin</th></tr><tr title="table-row"><a name="en0056"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black">Outcome \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0057"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black">(<span class="elsevierStyleItalic">n</span> = 10) \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0058"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black">(<span class="elsevierStyleItalic">n</span> = 10) \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0059"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">p-</span>Value<a class="elsevierStyleCrossRef" href="#tb4fn1"><span class="elsevierStyleSup">a</span></a> \t\t\t\t\t\t\n \t\t\t\t\t\t</th><a name="en0060"></a><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="top" scope="col" style="border-bottom: 2px solid black">95% CI<a class="elsevierStyleCrossRef" href="#tb4fn2"><span class="elsevierStyleSup">b</span></a> \t\t\t\t\t\t\n \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><a name="en0061"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top"><span class="elsevierStyleItalic">C. difficile</span> diarrhea \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0062"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">1 (10) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0063"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">2 (20) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0064"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">>0.99 \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0065"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">– \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0066"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">Febrile Neutropenia \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0067"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">5 (50) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0068"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">4 (40) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0069"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">>0.99 \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0070"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">– \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0071"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">CPE colonization \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0072"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">0 (0) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0073"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">1 (10) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0074"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">>0.99 \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0075"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">– \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><a name="en0076"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">AEs related to levofloxacin \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0077"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">– \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0078"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">3 (30) \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0079"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">– \t\t\t\t\t\t\n \t\t\t\t</td><a name="en0080"></a><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="top">6.7 – 65.2 \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] ] ] "notaPie" => array:2 [ 0 => array:3 [ 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Year/Month | Html | Total | |
---|---|---|---|
2024 October | 23 | 21 | 44 |
2024 September | 68 | 27 | 95 |
2024 August | 56 | 32 | 88 |
2024 July | 69 | 38 | 107 |
2024 June | 45 | 33 | 78 |
2024 May | 42 | 33 | 75 |
2024 April | 64 | 39 | 103 |
2024 March | 47 | 39 | 86 |
2024 February | 47 | 38 | 85 |
2024 January | 51 | 28 | 79 |
2023 December | 83 | 54 | 137 |
2023 November | 81 | 51 | 132 |
2023 October | 80 | 63 | 143 |
2023 September | 83 | 75 | 158 |
2023 August | 43 | 45 | 88 |
2023 July | 60 | 39 | 99 |
2023 June | 86 | 26 | 112 |
2023 May | 119 | 67 | 186 |
2023 April | 59 | 44 | 103 |
2023 March | 22 | 27 | 49 |
2023 February | 1 | 2 | 3 |